The main objective of this review is to provide an appraisal of the current status of the relationship between energy intake and the life span of animals. The concept that a reduction in food intake, or caloric restriction (CR), retards the aging process, delays the age-associated decline in physiological fitness, and extends the life span of organisms of diverse phylogenetic groups is one of the leading paradigms in gerontology. However, emerging evidence disputes some of the primary tenets of this conception. One disparity is that the CR-related increase in longevity is not universal and may not even be shared among different strains of the same species. A further misgiving is that the control animals, fed ad libitum (AL), become overweight and prone to early onset of diseases and death, and thus may not be the ideal control animals for studies concerned with comparisons of longevity. Reexamination of body weight and longevity data from a study involving over 60,000 mice and rats, conducted by a National Institute on Aging-sponsored project, suggests that CR-related increase in life span of specific genotypes is directly related to the gain in body weight under the AL feeding regimen. Additionally, CR in mammals and "dietary restriction" in organisms such as Drosophila are dissimilar phenomena, albeit they are often presented to be the very same. The latter involves a reduction in yeast rather than caloric intake, which is inconsistent with the notion of a common, conserved mechanism of CR action in different species. Although specific mechanisms by which CR affects longevity are not well understood, existing evidence supports the view that CR increases the life span of those particular genotypes that develop energy imbalance owing to AL feeding. In such groups, CR lowers body temperature, rate of metabolism, and oxidant production and retards the age-related pro-oxidizing shift in the redox state.

译文

本综述的主要目的是对能量摄入与动物寿命之间关系的现状进行评估。减少食物摄入量或热量限制 (CR) 会延缓衰老过程,延迟与年龄相关的生理适应性下降并延长各种系统发育群体的生物寿命的概念是主要范例之一在老年学中。然而,新出现的证据对这一概念的一些主要原则提出了质疑。一个差异是,与CR相关的寿命增加并不普遍,甚至可能不在同一物种的不同品系之间共享。另一个令人不安的是,随意喂食 (AL) 的对照动物变得超重,容易早发疾病和死亡,因此可能不是与寿命比较有关的研究的理想对照动物。由美国国家老龄研究所赞助的项目进行的一项涉及60,000多只小鼠和大鼠的研究的体重和寿命数据的重新检查表明,与CR相关的特定基因型寿命的增加与体重的增加直接相关在AL喂养方案下。此外,哺乳动物中的CR和果蝇等生物中的 “饮食限制” 是不同的现象,尽管它们通常被认为是相同的。后者涉及减少酵母而不是热量摄入,这与不同物种中常见的,保守的CR作用机制的概念不一致。尽管CR影响寿命的具体机制尚不清楚,但现有证据支持以下观点: CR会增加那些由于AL喂养而导致能量失衡的特定基因型的寿命。在这些组中,CR会降低体温,新陈代谢速率和氧化剂产生,并延缓氧化还原状态下与年龄相关的促氧化转变。

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